EP0377430A1 - Procédé de séparation des acides à partir de substrats contenant des sels et des hydrocarbures - Google Patents

Procédé de séparation des acides à partir de substrats contenant des sels et des hydrocarbures Download PDF

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Publication number
EP0377430A1
EP0377430A1 EP89890323A EP89890323A EP0377430A1 EP 0377430 A1 EP0377430 A1 EP 0377430A1 EP 89890323 A EP89890323 A EP 89890323A EP 89890323 A EP89890323 A EP 89890323A EP 0377430 A1 EP0377430 A1 EP 0377430A1
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EP
European Patent Office
Prior art keywords
acid
acids
resins
ion exchange
exchange resins
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP89890323A
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German (de)
English (en)
Inventor
Robert Edlauer
August E. Dipl.-Ing. Kirkovits
Ronald Dr. Westermayer
Otto Dipl.-Ing. Stojan
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Jungbunzlauer Austria AG
Original Assignee
Jungbunzlauer Austria AG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Jungbunzlauer Austria AG filed Critical Jungbunzlauer Austria AG
Publication of EP0377430A1 publication Critical patent/EP0377430A1/fr
Withdrawn legal-status Critical Current

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/42—Separation; Purification; Stabilisation; Use of additives
    • C07C51/47—Separation; Purification; Stabilisation; Use of additives by solid-liquid treatment; by chemisorption

Definitions

  • the invention relates to a method for separating acids from substrates containing salt and carbohydrates, in which the substrates are passed over resins which remove the acids from the substrate by adsorption, and the acids are then separated from the resins by elution.
  • organic and inorganic acids are used: in applications in the pharmaceutical and food sector, but also when used in cleaning chemicals, these have to be of a particularly high quality.
  • liquid / liquid extraction and the formation of volatile derivatives have also been proposed as cleaning methods for acids. All of these methods are used in the treatment of technically important acids such as Lactic acid, malic acid, succinic acid, tartaric acid, citric acid, gluconic acid and phosphoric acid can also be used on an industrial scale.
  • the cleaning methods which isolate the acid from an insoluble salt, consume large amounts of auxiliary chemicals. In most cases, a poorly soluble calcium salt is formed, which is then reacted with sulfuric acid to form the free acid and an equimolar amount of gypsum.
  • the present invention is based on the prior art, which is given by US Pat. No. 4,720,579.
  • the basic principle here is to pass substrates containing acids, salts and carbohydrates over resins which act selectively as adsorbers for the acids, while the other constituents of the substrates pass through.
  • the acids whose purification or extraction is concerned are then obtained by elution of the loaded resins.
  • the acids are selectively and reversibly adsorbed and the cleaning effects achieved and the loadability of the resins are significantly higher than those of the nonionic resins.
  • the process according to the invention for the chromatographic purification or separation of acids is primarily characterized in that basic ion exchange resins are used for the separation.
  • DD-PS 203 533 describes an ion exchange process for the recovery of carboxylic and oxycarboxylic acids from their salt solutions containing foreign salts, in which the salts are first converted into acids via cation exchangers in the Hent form. A mixture of carboxylic acids and foreign acids is obtained. A less concentrated fraction of this mixture is then loaded into an anion exchanger which is initially in the base or hydroxyl form, that is to say essentially converted into the carboxylic acid form. A more highly concentrated fraction of the acid mixture obtained in the decationization stage is then passed over the acid-laden ion exchanger, the acid to be obtained passing unhindered through the resin bed and only the stronger foreign anions (chloride being mentioned) being bound to the resin by ion exchange.
  • DE-OS 29 31 759 relates to the separation of citric acid from a Mixture with oxalic acid and nitric acid, in which this mixture is passed through an anion exchanger, which may have been previously equilibrated with citric acid.
  • the ion exchanger extracts the nitric acid and the oxalic acid from this mixture by ion exchange while the citric acid passes through the column.
  • DE-OS 25 43 332 relates to a process for separating the maleic acid contamination from synthetic tartaric acid, in which it is passed over basic anion exchangers which are in hydroxyl or tartrate form. Again, the ion exchanger removes the stronger maleic acid from the mixture by ion exchange, and the tartaric acid to be extracted passes through the column.
  • the acids to be obtained or purified are not bound to the resins by ion exchange, but are adsorptively bound and obtained from there by elution.
  • the resins are preferably used in acid-laden form.
  • the resin is advantageously loaded with an anion to which the resin has the same or a higher affinity than the acid to be purified.
  • the loading of the resin does not have to be carried out as an explicit operation, in many cases it arises by itself through prolonged use.
  • basic ion exchange resins loaded with hydrochloric, nitric, phorphoric, citric or sulfuric acid, preferably with sulfuric acid, are used.
  • the anion exchange resins according to the invention can be of a strong or weakly basic nature in the form of a gel or macroreticular.
  • the ion exchangers can have a styrene / divinylbenzene base or a crosslinked acrylic resin base.
  • the elution can be carried out with water; is preferred however, a dilute acid, especially sulfuric acid, is used in a concentration range of 0 to 1%. As is known, low pH values can also be set favorably in the process of the invention.
  • the elution temperature can be selected between room temperature and the stability limit temperature of the resin, preferably the elution takes place at a temperature which prevents microbial contamination of the resin.
  • the process is preferably carried out in a quasi-continuous apparatus (simulated moving bed), but fully continuous or batch procedures are also possible.
  • the anion exchange resins were brought into the sulfate form with 4% NaOH with 10% sulfuric acid and conditioned with 0.1% sulfuric acid.
  • the resins prepared in this way were filled into columns with a diameter of 25 mm and a length of 800 mm.
  • 0.1% sulfuric acid was eluted with 15 ml / min.
  • the column temperature was set to 80 ° C with a circulation thermostat.
  • the eluate concentrations were determined by measuring the refractive index. Under these conditions, maltose and citric acid were completely separated on almost all resins.
  • the table shows the retention volumes of maltose and citric acid.
  • Example 2 As in Example 1, a column was packed with AMBERLITE IRA 67 and equilibrated with a flow of 30 ml / min with 0.1% sulfuric acid. The temperature of the column was set at 75 ° C. The exclusion volume of the resin was determined by injection of 1 ml of a 5% dextran T10 solution. It can be assumed that a high molecular weight, uncharged substance will not be retained under these conditions. The Exclusion volume was calculated as follows: T tr retention time dextran in seconds V column volume in ml Fl flow in ml.s ⁇ 1
  • Example 2 was repeated at a temperature of 60 ° C. substance concentration Separator number Partition coefficient [Weight%] n K Sodium sulfate 10th 7.70 0.192 30th 8.71 0.242 Maltose 10th 1.62 0.110 40 1.70 0.112 glucose 10th 4.93 0.322 40 4.57 0.312 Gluconic acid 10th 5.33 0.489 40 4.85 0.483 citric acid 10th 13.83 1,743 40 12.69 1,617
  • Example 2 was repeated at a temperature of 90 ° C. substance concentration Separator number Partition coefficient [Weight%] n K Sodium sulfate 10th 11.09 0.227 30th 12.39 0.280 Maltose 10th 2.97 0.183 40 3.06 0.186 glucose 10th 8.76 0.404 40 8.22 0.392 Gluconic acid 10th 10.96 0.628 40 9.80 0.594 Lactic acid 10th 18.99 0.776 40 17.77 0.752 citric acid 10th 30.00 2,514 40 10/25 2,147
  • a polypropylene column 27 mm in diameter and 146 mm in length was packed with Amberlite IRA-67 in the sulfate form. 4.97 ml / min of 0.1% sulfuric acid were pumped over the column at a temperature of 28 ° C. 0.5 ml of hydrofluoric acid or phosphoric acid were then injected into the eluent stream. The leakage of the substances from the column was measured using a conductivity detector. substance concentration Separator number Partition coefficient [Weight%] n K Hydrofluoric acid 10th 15.45 1.06 phosphoric acid 40 January 15 3.14 This example demonstrates the possibility of cleaning inorganic acids as well.
  • Example 2 was repeated with 0.1% sulfuric acid as eluent and IRA900 as ion exchanger at a temperature of 75 ° C.
  • substance concentration Separator number Partition coefficient [Weight%] n K Sodium sulfate 10th 6.80 0.319 30th 8.01 0.358 Maltose 10th 2.77 0.316 40 2.77 0.309 glucose 10th 6.24 0.485 40 6.24 0.485 Gluconic acid 10th 7.02 0.726 40 6.43 0.717 Lactic acid 10th 16.73 1,036 40 16.41 1,043 Tartaric acid 10th 19.74 2,909 Malic acid 10th 16.86 2,212 Itaconic acid 10th 15.96 3,095
  • Example 2 was repeated with water as the eluent and IRA900 as the ion exchanger at a temperature of 75 ° C.
  • a semi-continuous chromatography system consisting of 10 columns (diameter 25 mm, length 1600 mm) was filled with AMBERLITE IRA 900 in the Suflat form.
  • the system is constructed so that the columns are connected to a ring by pipes. This ring line is connected between the columns via valves on four supply lines. These supply lines are raw product entry, eluent entry, product outlet and raffinate outlet.
  • the flows in the system are kept constant by means of adjustable piston pumps.
  • exactly four valves are always open and divide the ring formed from columns into four zones. These zones are switched by a process computer by one column in the direction of flow after predetermined times. These switching processes simulate a resin flow against the flow direction, which is why it is referred to in the literature as "simulated moving called "bed” process.
  • the zoo was divided according to the following scheme: Zone 1 2 pillars Zone 2 3 pillars Zone 3 4 columns Zone 4 1 pillar 8 ml of crude product and 32 ml of water were fed in per minute and 16 ml of product or 24 ml of raffinate were removed.
  • the temperature of the plant was kept constant at 70 ° C.
  • the internal circulation in the column ring was set to 4 ml / min.
  • the valves were switched every 1550 seconds.
  • a lactic acid fermentation maize concentrated to about 40% was fed into this plant.
  • a purified lactic acid was obtained with a yield of over 95%.
  • the raffinate contained above all polymers which can severely disrupt the production of lactic acid.
  • the cleaning effect is also high chemical oxygen demand of the raffinate of 13.5 g / l is shown.
  • the lactic acid before and after the chromatographic separation was compared in the following table: in front to Lactic acid [%] 40.52 19.53 Color [405nm.1cm] 1.94 0.43 Sulfate [%] 1.78 0.03 Chloride [mg / kg] 330 23 Sodium [mg / kg] 7820 330 Magnesium [mg / kg] 7 0 Iron [mg / kg] 27th 5
  • a semi-technical chromatography system consisting of twelve columns (diameter 0.5 m, length 2.0 m) was filled with Amberlite IRA-67. The resin was brought into the sulfate form by rinsing with 0.1% sulfuric acid. The columns were connected as shown in the diagram below.
  • the productivity of the plant is 2.86 t of citric acid anhydrate per day, the yield of 99.9% is much better than that of the already known cleaning processes for citric acid. It can be clearly seen that almost all impurities, whether cationic, anionic or uncharged, are separated.
  • Example 9 was repeated with crude phosphoric acid.
  • a pre-filtered wet phosphoric acid (green acid) with a concentration vib 37% P2O5 was fed.
  • the column was switched every 1500 seconds.
  • the analysis of the product and raffinate samples in the equilibrium state showed the following values: product Raffinate titratable acid as P2O5 15.60 1.90% Color (405nm.1cm) 0.047 1,486
  • the phosphoric acid yield was 89.9%, a comparison of the cation load before and after the chromatographic separation shows the high cleaning performance of the system (all concentrations based on 100% P2O5).
  • magnesium 20800 42 mg / kg calcium 358 9 mg / kg aluminum 3390 410 mg / kg iron 4620 1200 mg / kg zinc 855 15 mg / kg chrome 614 102 mg / kg copper 29 0 mg / kg nickel 56 0 mg / kg manganese 21st 0 mg / kg cadmium 23 0 mg / kg

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Treatment Of Liquids With Adsorbents In General (AREA)
EP89890323A 1989-01-05 1989-12-18 Procédé de séparation des acides à partir de substrats contenant des sels et des hydrocarbures Withdrawn EP0377430A1 (fr)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
AT23/89 1989-01-05
AT2389 1989-01-05
AT2773/89 1989-12-06
AT277389 1989-12-06

Publications (1)

Publication Number Publication Date
EP0377430A1 true EP0377430A1 (fr) 1990-07-11

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Country Status (2)

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EP (1) EP0377430A1 (fr)
CA (1) CA2007126A1 (fr)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0483831A3 (en) * 1990-11-02 1993-01-13 Mitsubishi Kasei Corporation Process for separating an organic acid or acids from an organic acid-containing solution
US5786185A (en) * 1991-09-13 1998-07-28 Reilly Industries, Inc. Process for producing and recovering lactic acid
US5965771A (en) * 1997-10-03 1999-10-12 The Regents Of The University Of California Regeneration of carboxylic acid-laden basic sorbents by leaching with a volatile base in an organic solvent
NL1010090C2 (nl) * 1998-09-15 2000-03-17 Gerard Kessels Sociedad Anonim Werkwijze voor de bereiding van 2- en 4-hydroxyamandelzuur.
US6114577A (en) * 1995-02-15 2000-09-05 Reilly Industries, Inc. Desorption process and apparatus
FR2900654A1 (fr) * 2006-05-05 2007-11-09 Applexion Procede de purification d'un acide organique par chromatographie
DE102016001070A1 (de) 2015-02-06 2016-08-11 Rwth Aachen Verfahren zur Trennung organischer Dicarbonsäuren durch Adsorption hydrophober poröser Materialien
WO2017095686A1 (fr) * 2015-12-01 2017-06-08 Dow Global Technologies Llc Séparation chromatographique d'acides organiques utilisant une résine présentant une capacité d'échange d'anions à base forte et faible

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104744241A (zh) * 2013-12-30 2015-07-01 中粮营养健康研究院有限公司 一种从柠檬酸发酵液中提纯柠檬酸的方法

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2664441A (en) * 1951-07-19 1953-12-29 Harry S Owens Separation of organic acids
US2697725A (en) * 1950-03-18 1954-12-21 Sharples Corp Recovery of organic acids from aqueous solutions
FR1194165A (fr) * 1959-11-06
CH523861A (de) * 1967-05-22 1972-06-15 Sun Oil Co Verfahren zur Gewinnung von Carbonsäuren
JPS52156814A (en) * 1976-06-21 1977-12-27 Tokuyama Soda Co Ltd Purification of tartaric acid

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR1194165A (fr) * 1959-11-06
US2697725A (en) * 1950-03-18 1954-12-21 Sharples Corp Recovery of organic acids from aqueous solutions
US2664441A (en) * 1951-07-19 1953-12-29 Harry S Owens Separation of organic acids
CH523861A (de) * 1967-05-22 1972-06-15 Sun Oil Co Verfahren zur Gewinnung von Carbonsäuren
JPS52156814A (en) * 1976-06-21 1977-12-27 Tokuyama Soda Co Ltd Purification of tartaric acid

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
CHEMICAL ABSTRACTS, Band 83, Nr. 23, 5. Juni 1978, Zusammenfassung Nr. 169603b, Columbus, Ohio, US; & JP-A-77 156 814 (TOKUYAMA SODA CO., LTD) 27-12-1977 *

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0483831A3 (en) * 1990-11-02 1993-01-13 Mitsubishi Kasei Corporation Process for separating an organic acid or acids from an organic acid-containing solution
US5245078A (en) * 1990-11-02 1993-09-14 Mitsubishi Kasei Corporation Process for separating an organic acid or acids from an organic acid-containing solution
US5786185A (en) * 1991-09-13 1998-07-28 Reilly Industries, Inc. Process for producing and recovering lactic acid
US6114577A (en) * 1995-02-15 2000-09-05 Reilly Industries, Inc. Desorption process and apparatus
US5965771A (en) * 1997-10-03 1999-10-12 The Regents Of The University Of California Regeneration of carboxylic acid-laden basic sorbents by leaching with a volatile base in an organic solvent
NL1010090C2 (nl) * 1998-09-15 2000-03-17 Gerard Kessels Sociedad Anonim Werkwijze voor de bereiding van 2- en 4-hydroxyamandelzuur.
EP0987245A1 (fr) * 1998-09-15 2000-03-22 Gerard Kessels S.A. Procédé pour la préparation de l'acide 2- et 4-hydroxy-mandélique
FR2900654A1 (fr) * 2006-05-05 2007-11-09 Applexion Procede de purification d'un acide organique par chromatographie
WO2007128918A1 (fr) * 2006-05-05 2007-11-15 Applexion Procede de purification d'un acide organique par chromatographie
DE102016001070A1 (de) 2015-02-06 2016-08-11 Rwth Aachen Verfahren zur Trennung organischer Dicarbonsäuren durch Adsorption hydrophober poröser Materialien
WO2016124170A1 (fr) 2015-02-06 2016-08-11 Rwth Aachen Procédé de séparation d'acides dicarboxyliques organiques par adsorption de matériaux poreux hydrophobes
WO2017095686A1 (fr) * 2015-12-01 2017-06-08 Dow Global Technologies Llc Séparation chromatographique d'acides organiques utilisant une résine présentant une capacité d'échange d'anions à base forte et faible

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Publication number Publication date
CA2007126A1 (fr) 1990-07-05

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